Product Details

SNP ID
rs201338298
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.4:51994854 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
ATCAGGCACTGCCTCTTCAGTCTTG[C/T]TCCTTGCACTCTCTGAACTTATGGA
Phenotype
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
LRRC66 PubMed Links

Gene Details

Gene
LRRC66
Gene Name
leucine rich repeat containing 66
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001024611.2 3902 Missense Mutation AAC,AGC N723S NP_001019782.1
XM_011534383.2 3902 Missense Mutation AAC,AGC N775S XP_011532685.1
XM_017008162.1 3902 Missense Mutation AAC,AGC N487S XP_016863651.1

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